A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158985



Internal ID20726025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79162139..79162612hg38UCSC Ensembl
chr7:78791455..78791928hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607221
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0007


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer